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2-year follow-up of Nevo RES-elution I, a randomisedmulticentre comparison of the Nevo Sirolimus-eluting coronarystent system using RES technology with the Taxus LibertéPaclitaxel-eluting stent
Fajadet, J; Abizaid, A; Ormiston, J; Schofer, J; Mauri, L; Verheye, S; Stoll, H. P; Macours, N; Christian, S.
Afiliação
  • Fajadet, J; Clinique Pasteur de Toulouse. Toulouse. FR
  • Abizaid, A; Instituto Dante Pazzanese de Cardiologia. Sao Paulo. BR
  • Ormiston, J; Auckland City Hospital. Auckland. NZ
  • Schofer, J; Herzkatheterlabor und Praxisklinik. Hamburg. DE
  • Mauri, L; Harvard Clinical Research Institute. Boston. US
  • Verheye, S; AZ Middelheim. Antuerpia. BE
  • Stoll, H. P; Cordis Clinical Research. Bridgewater. US
  • Macours, N; Cordis Clinical Research. Waterloo. BE
  • Christian, S; Cordis Clinical Research. Waterloo. BE
EuroIntervention ; 07: 1-2, 2014.
Article em En | SES-SP, SESSP-IDPCPROD, SES-SP | ID: biblio-1062675
Biblioteca responsável: BR79.1
Localização: BR79.1
ABSTRACT

Aims:

The NEVO™ sirolimus eluting coronary stent is designed to improvelong-term PCI safety by combining sirolimus release from reservoirs withbioabsorbable polymer to reduce spatial and temporal polymer exposure.Absorption of drug and polymer within approximately three months limits theduration of vessel wall exposure to the polymer. Thereafter, only a biologically inertbare-metal platform remains. The NEVO™ stent was first evaluated in the multicenterrandomised NEVO RES-Elution I trial which demonstrated its superiority tothe TAXUS Liberté Paclitaxel - eluting stent.
Assuntos
Texto completo: 1 Base de dados: SES-SP / SESSP-IDPCPROD Assunto principal: Stents / Constrição Patológica / Sirolimo Idioma: En Ano de publicação: 2014
Texto completo: 1 Base de dados: SES-SP / SESSP-IDPCPROD Assunto principal: Stents / Constrição Patológica / Sirolimo Idioma: En Ano de publicação: 2014